Ono Y, Manabe Y, Sakai K, Hayashi Y, Abe K
Department of Neurology, National Hospital Organization, Okayama Medical Center, 1711-1 Tamasu, Okayama, Japan.
J Neurol Sci. 2006 Dec 21;251(1-2):107-9. doi: 10.1016/j.jns.2006.09.009. Epub 2006 Nov 9.
We report a very rare case of Japanese encephalitis (JE) presenting with reversible stereotyped movement in the subacute stage. A 58-year-old woman presented with high fever, headache, nausea, vomiting, and consciousness disturbance. Cranial magnetic resonance imaging (MRI) of fluid attenuated inversion recovery (FLAIR) and T2-weighted image (WI) showed high intensity areas in the bilateral thalamus, caudate nucleus and hippocampus. She developed coma, convulsion, and ballism in the acute stage. One month after onset, she showed rhythmic, stereotyped, repetitive movements with hypoperfusion in the thalamus and frontal cortex on single photon emission computed tomography (SPECT). Three months later, her stereotyped movement improved accompanied by recovery of hypoperfusion in the thalamus and frontal cortex on SPECT. We speculated that her stereotyped movement was clonic perseveration due to frontal dysfunction induced by thalamofrontal disconnection.
我们报告了一例非常罕见的日本脑炎(JE)病例,其在亚急性期出现可逆性刻板运动。一名58岁女性出现高热、头痛、恶心、呕吐及意识障碍。液体衰减反转恢复序列(FLAIR)和T2加权像(WI)的头颅磁共振成像(MRI)显示双侧丘脑、尾状核和海马区有高强度信号区。急性期她出现昏迷、惊厥和舞蹈症。发病一个月后,单光子发射计算机断层扫描(SPECT)显示她出现节律性、刻板、重复性运动,同时丘脑和额叶皮质灌注不足。三个月后,她的刻板运动有所改善,SPECT显示丘脑和额叶皮质灌注不足情况恢复。我们推测她的刻板运动是由于丘脑额叶连接中断导致额叶功能障碍引起的阵挛性持续状态。